GLP/GCLP Quality Assurance Auditor
Date: Aug 2, 2022
Location: Netanya, IL, 11
Company: Teva Pharmaceuticals
Who are we?
Job Description
TEVA's Global R&D unit is looking for GLP/GCLP Quality Assurance Auditor, for a challenging role in Abic site in Netanya for.
The position includes Involvement in Non-Clinical and Bioanalytical QA related activities that are planned and performed to assure quality and compliance with global and local procedures, relevant regulations, through regulated studies, documents and non-clinical sites.
• Participate in conduct GLP site audits
• Participate in conduct of study protocol audit, amendments, raw data and reports and other audits in the support of a GLP/GCLP studies.
• Participate in conduct of process and study based audits at a GLP/GCLP Laboratory in support of regulated studies.
• Participate in conduct of facility prequalification/qualification audits at Contract Research Organizations (CROs).
• To issue QA Audit Reports for the different audit activities
• To participate in SOPs, work instructions, forms and templates development and review
• Participate in review of non-clinical parts of regulatory submissions (e.g. INDs, IBs).
• Support GLP training activities
• Support inspection readiness activites
Temporary position replacement for maternity leave
Qualifications
• Life Sciences background at least Bsc. level.
• Experience as an auditor - An advantage
• Professional experience in laboratory work specializing in biological experiments, Bioassays, or GLP research facility
• Ability to work independently as well as to effectively communicate and collaborate in a team environment
• Extensive experience with computer software usages
• Fluent English- Must
Function
Sub Function
Reports To
Senior Director GLP/GCLP Quality, Global QA
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